| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:90362787-90363004 | Rare:42 | ||||
| chr13:90415359-90415430 | Common:1; Rare:18 | ||||
| chr13:90594800-90594977 | Rare:28 | ||||
| chr13:90684085-90684121 | Rare:6 | ||||
| chr13:91347505-91348099 | Common:2; Rare:209 | ||||
| chr13:91348121-91348643 | Common:1; Rare:176 | ||||
| chr13:91348656-91349206 | Common:5; Rare:205 | ||||
| chr13:91350613-91350618 | |||||
| chr13:91351075-91351361 | Common:1; Rare:91 | ||||
| chr13:93217753-93218043 | Rare:57 | ||||
| chr13:93227442-93227727 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:93227964-93228158 | Common:1; Rare:49 | ||||
| chr13:93228351-93228700 | Rare:95 | ||||
| chr13:93244302-93244562 | Rare:41 | ||||
| chr13:93244679-93244813 | Common:4; Rare:22 |